Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - Springer
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …